JOP20180012A1 - Sulfonylation process using nonafluorobutanesulfonyl fluoride - Google Patents
Sulfonylation process using nonafluorobutanesulfonyl fluorideInfo
- Publication number
- JOP20180012A1 JOP20180012A1 JOP/2018/0012A JOP20180012A JOP20180012A1 JO P20180012 A1 JOP20180012 A1 JO P20180012A1 JO P20180012 A JOP20180012 A JO P20180012A JO P20180012 A1 JOP20180012 A1 JO P20180012A1
- Authority
- JO
- Jordan
- Prior art keywords
- nonafluorobutanesulfonyl fluoride
- sulfonylation process
- sulfonylation
- nonafluorobutanesulfonyl
- fluoride
- Prior art date
Links
Classifications
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- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/30—Oxygen atoms, e.g. delta-lactones
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
- C07D451/06—Oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/12—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
- C07D493/18—Bridged systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
Abstract
The present invention is directed to a process for the preparation of a compound of formula (XX)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261680446P | 2012-08-07 | 2012-08-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
JOP20180012A1 true JOP20180012A1 (en) | 2019-01-30 |
Family
ID=48980367
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JOP/2018/0012A JOP20180012A1 (en) | 2012-08-07 | 2012-08-07 | Sulfonylation process using nonafluorobutanesulfonyl fluoride |
JOP/2013/0237A JO3248B1 (en) | 2012-08-07 | 2013-08-06 | Process for the preparation of c-fms kinase inhibitors |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JOP/2013/0237A JO3248B1 (en) | 2012-08-07 | 2013-08-06 | Process for the preparation of c-fms kinase inhibitors |
Country Status (13)
Country | Link |
---|---|
US (2) | US9029352B2 (en) |
EP (2) | EP3091006B1 (en) |
JP (1) | JP6290884B2 (en) |
CN (2) | CN104520295B (en) |
AR (2) | AR092070A1 (en) |
AU (2) | AU2013299926B2 (en) |
ES (2) | ES2658773T3 (en) |
HK (2) | HK1209418A1 (en) |
IN (1) | IN2015DN00660A (en) |
JO (2) | JOP20180012A1 (en) |
TW (2) | TWI646090B (en) |
UY (1) | UY34972A (en) |
WO (1) | WO2014025679A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201811326A (en) | 2016-07-18 | 2018-04-01 | 比利時商健生藥品公司 | Salt forms of 4-cyano-N-(2-(4,4-dimethylcyclohex-1-en-1-yl)-6-(2,2,6,6-tetramethyltetrahydro-2H-pyran-4-yl)pyridin-3-yl)-1H-imidazole-2-carboxamide |
TWI752980B (en) * | 2016-07-18 | 2022-01-21 | 比利時商健生藥品公司 | Crystalline forms of 4-cyano-n-(2-(4,4-dimethylcyclohex-1-en-1-yl)-6-(2,2,6,6-tetramethyltetrahydro-2h-pyran-4-yl)pyridin-3-yl)-1h-imidazole-2-carboxamide |
JP6831558B2 (en) * | 2016-08-23 | 2021-02-17 | 株式会社Hbcフナト | Brain function improving composition |
JP2020510673A (en) * | 2017-03-03 | 2020-04-09 | ヤンセン バイオテツク,インコーポレーテツド | Combination therapy comprising a small molecule CSF-1R inhibitor and an agonistic antibody specifically binding to CD40 for the treatment of cancer |
WO2020222109A1 (en) | 2019-05-02 | 2020-11-05 | Janssen Biotech, Inc. | Csf-1/csf-1r gene set |
Family Cites Families (95)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2466420A (en) | 1947-11-26 | 1949-04-05 | Eastman Kodak Co | Ketene condensation products with aldehydes |
US3226394A (en) | 1964-06-16 | 1965-12-28 | Shulton Inc | Pyridylethylated anthranilamides and derivatives thereof |
CH504416A (en) | 1966-12-05 | 1971-03-15 | Ciba Geigy Ag | Aromatic sulphamoyl cpd prepn. |
US4551540A (en) | 1983-01-17 | 1985-11-05 | Borg-Warner Chemicals, Inc. | Substituted 2,5-dimethylpyrroles |
US5190541A (en) | 1990-10-17 | 1993-03-02 | Boston Scientific Corporation | Surgical instrument and method |
ATE239506T1 (en) | 1992-03-05 | 2003-05-15 | Univ Texas | USE OF IMMUNOCONJUGATES FOR THE DIAGNOSIS AND/OR THERAPY OF VASCULARIZED TUMORS |
US5474765A (en) | 1992-03-23 | 1995-12-12 | Ut Sw Medical Ctr At Dallas | Preparation and use of steroid-polyanionic polymer-based conjugates targeted to vascular endothelial cells |
US5686472A (en) | 1992-10-29 | 1997-11-11 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US5593992A (en) | 1993-07-16 | 1997-01-14 | Smithkline Beecham Corporation | Compounds |
JPH10507185A (en) | 1994-10-14 | 1998-07-14 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | 2- (Imidazol-4-yl) carbapenem derivatives, their intermediates and use as antibacterial agents |
CA2216943C (en) | 1995-04-19 | 2003-06-17 | Schneider (Usa) Inc. | Drug release coated stent |
US6117432A (en) | 1995-04-20 | 2000-09-12 | Societe D'exploitation De Produits Pour Les Industries Chimiques (S.E.P.P.I.C.) | Therapeutic composition comprising an antigen or an in vivo generator of a compound comprising an amino acid sequence |
TW349948B (en) | 1995-10-31 | 1999-01-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 2-quinolone derivatives |
GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
SI1162201T1 (en) | 1995-12-08 | 2006-08-31 | Janssen Pharmaceutica Nv | Farnesyl protein transferase inhibiting (imidazol-5-yl)methyl-2-quinolinone derivatives |
US5874442A (en) | 1995-12-22 | 1999-02-23 | Schering-Plough Corporation | Tricyclic amides useful for inhibition of G-protein function and for treatment of proliferative disease |
US6011029A (en) | 1996-02-26 | 2000-01-04 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
US5702390A (en) | 1996-03-12 | 1997-12-30 | Ethicon Endo-Surgery, Inc. | Bioplar cutting and coagulation instrument |
US5900484A (en) * | 1996-09-18 | 1999-05-04 | Lonza Ag | Process for the preparation of arylamides of heteroaromatic carboxylic acids |
EP0923557A4 (en) | 1996-08-09 | 1999-12-08 | Merck & Co Inc | Stereoselective deoxygenation reaction |
JP2001505548A (en) | 1996-12-20 | 2001-04-24 | トヴァリシェストヴォ エス オグラニチェンノイ オトヴェトストヴェンノストジュ“タブジュファーム” | Method and apparatus for producing freeze-dried hydrochloride-1β, 10β-epoxy-13-dimethylamino-guaia-3 (4) -ene-6,12-olide |
UA59384C2 (en) | 1996-12-20 | 2003-09-15 | Пфайзер, Інк. | Preventing bone mass loss and recovery thereof by means of prostaglandin agonists |
TW591030B (en) | 1997-03-10 | 2004-06-11 | Janssen Pharmaceutica Nv | Farnesyl transferase inhibiting 1,8-annelated quinolinone derivatives substituted with N- or C-linked imidazoles |
CA2288140C (en) | 1997-04-25 | 2007-04-03 | Janssen Pharmaceutica N.V. | Farnesyltransferase inhibiting quinazolinones |
TW491872B (en) | 1997-05-27 | 2002-06-21 | Ciba Sc Holding Ag | Block oligomers containing l-hydrocarbyloxy-2,2,6,6-tetramethyl-4- piperidyl groups as stabilizers for lower polyolefin |
US6100254A (en) | 1997-10-10 | 2000-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of protein tyrosine kinases |
ATE220278T1 (en) | 1998-03-05 | 2002-07-15 | Formula One Administration Ltd | DATA TRANSMISSION SYSTEM |
US6303654B1 (en) | 1998-03-12 | 2001-10-16 | Wisconsin Alumni Research Foundation | Acyclic monoterpenoid derivatives |
WO2000001691A1 (en) | 1998-07-01 | 2000-01-13 | Merck & Co., Inc. | Process for making farnesyl-protein transferase inhibitors |
EP1097147A4 (en) | 1998-07-10 | 2001-11-21 | Merck & Co Inc | Novel angiogenesis inhibitors |
ES2237125T3 (en) | 1998-08-27 | 2005-07-16 | Pfizer Products Inc. | DERIVATIVES OF QUINOLIN-2-ONA USEFUL AS ANTICANCERIGEN AGENTS. |
JP3495706B2 (en) | 1998-08-27 | 2004-02-09 | ファイザー・プロダクツ・インク | Alkynyl-substituted quinolin-2-one derivatives useful as anticancer drugs |
GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
IL143859A0 (en) | 1998-12-23 | 2002-04-21 | Janssen Pharmaceutica Nv | 1,2-annelated quinoline derivatives |
JP4876239B2 (en) | 1999-01-11 | 2012-02-15 | プリンストン ユニバーシティー | High affinity inhibitors for target confirmation and use thereof |
US7125875B2 (en) | 1999-04-15 | 2006-10-24 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
BR0009721A (en) | 1999-04-15 | 2002-02-13 | Bristol Myers Squibb Co | Cyclic protein tyrosine kinase inhibitors |
CA2372053C (en) | 1999-04-28 | 2008-09-02 | Board Of Regents, The University Of Texas System | Compositions and methods for cancer treatment by selectively inhibiting vegf |
US6346625B1 (en) | 1999-06-23 | 2002-02-12 | Astrazeneca Ab | Protein kinase inhibitors |
DE19962924A1 (en) | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituted oxazolidinones and their use |
WO2001047921A1 (en) | 1999-12-28 | 2001-07-05 | Pharmacopeia, Inc. | Pyrimidine and triazine kinase inhibitors |
FR2803592A1 (en) | 2000-01-06 | 2001-07-13 | Aventis Cropscience Sa | NOVEL DERIVATIVES OF 3-HYDROXYPICOLINIC ACID, PROCESS FOR THEIR PREPARATION AND FUNGICIDAL COMPOSITIONS CONTAINING SAME |
US6558385B1 (en) | 2000-09-22 | 2003-05-06 | Tissuelink Medical, Inc. | Fluid-assisted medical device |
US6692491B1 (en) | 2000-03-24 | 2004-02-17 | Scimed Life Systems, Inc. | Surgical methods and apparatus for positioning a diagnostic or therapeutic element around one or more pulmonary veins or other body structures |
US6776796B2 (en) | 2000-05-12 | 2004-08-17 | Cordis Corportation | Antiinflammatory drug and delivery device |
AU2687702A (en) | 2000-10-17 | 2002-04-29 | Merck & Co Inc | Orally active salts with tyrosine kinase activity |
US7105682B2 (en) | 2001-01-12 | 2006-09-12 | Amgen Inc. | Substituted amine derivatives and methods of use |
TWI238824B (en) | 2001-05-14 | 2005-09-01 | Novartis Ag | 4-amino-5-phenyl-7-cyclobutyl-pyrrolo[2,3-d]pyrimidine derivatives |
US7101884B2 (en) | 2001-09-14 | 2006-09-05 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
WO2003024931A1 (en) | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
TWI259081B (en) | 2001-10-26 | 2006-08-01 | Sugen Inc | Treatment of acute myeloid leukemia with indolinone compounds |
PT1441737E (en) | 2001-10-30 | 2006-12-29 | Dana Farber Cancer Inst Inc | Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity |
CN1290844C (en) | 2001-12-27 | 2006-12-20 | 施万制药 | Indolinone derivatives |
CN100558715C (en) | 2002-05-23 | 2009-11-11 | 西托匹亚有限公司 | Kinases inhibitor |
AR037647A1 (en) | 2002-05-29 | 2004-12-01 | Novartis Ag | USED DIARILUREA DERIVATIVES FOR THE TREATMENT OF DEPENDENT DISEASES OF THE PROTEIN KINase |
MY141867A (en) | 2002-06-20 | 2010-07-16 | Vertex Pharma | Substituted pyrimidines useful as protein kinase inhibitors |
GB0215676D0 (en) | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
PL375447A1 (en) | 2002-08-14 | 2005-11-28 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors and uses thereof |
AU2003288899B2 (en) | 2002-08-23 | 2009-09-03 | Novartis Vaccines And Diagnostics, Inc. | Benzimidazole quinolinones and uses thereof |
WO2004022525A1 (en) | 2002-09-05 | 2004-03-18 | Neurosearch A/S | Amide derivatives and their use as chloride channel blockers |
US7208493B2 (en) | 2002-10-03 | 2007-04-24 | Targegen, Inc. | Vasculostatic agents and methods of use thereof |
AU2003280599A1 (en) | 2002-10-29 | 2004-05-25 | Kirin Beer Kabushiki Kaisha | QUINOLINE DERIVATIVES AND QUINAZOLINE DERIVATIVES INHIBITING AUTOPHOSPHORYLATION OF Flt3 AND MEDICINAL COMPOSITIONS CONTAINING THE SAME |
EP1565187A4 (en) | 2002-11-13 | 2010-02-17 | Novartis Vaccines & Diagnostic | Methods of treating cancer and related methods |
TWI335913B (en) | 2002-11-15 | 2011-01-11 | Vertex Pharma | Diaminotriazoles useful as inhibitors of protein kinases |
EP1581526B1 (en) | 2002-12-18 | 2009-03-11 | Vertex Pharmaceuticals Incorporated | Benzisoxazole derivatives useful as inhibitors of protein kinases |
MXPA05010945A (en) | 2003-04-09 | 2005-11-25 | Japan Tobacco Inc | Heteroaromatic pentacyclic compound and medicinal use thereof. |
MXPA05011503A (en) | 2003-04-25 | 2006-05-31 | Johnson & Johnson | C-fms kinase inhibitors. |
US20050113566A1 (en) | 2003-04-25 | 2005-05-26 | Player Mark R. | Inhibitors of C-FMS kinase |
US7427683B2 (en) | 2003-04-25 | 2008-09-23 | Ortho-Mcneil Pharmaceutical, Inc. | c-fms kinase inhibitors |
US7790724B2 (en) | 2003-04-25 | 2010-09-07 | Janssen Pharmaceutica N.V. | c-fms kinase inhibitors |
JP5013593B2 (en) | 2003-07-28 | 2012-08-29 | スミスクライン ビーチャム コーポレーション | Compound |
CN1950347B (en) | 2003-10-23 | 2012-04-04 | Ab科学公司 | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
GB0326601D0 (en) | 2003-11-14 | 2003-12-17 | Novartis Ag | Organic compounds |
WO2005073225A1 (en) | 2004-01-30 | 2005-08-11 | Ab Science | 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors |
AU2005299837A1 (en) | 2004-10-22 | 2006-05-04 | Janssen Pharmaceutica, N.V. | Inhibitors of c-fms kinase |
CN101084208A (en) * | 2004-10-22 | 2007-12-05 | 詹森药业有限公司 | Aromatic amides as inhibitors of c-fms kinase |
NZ555289A (en) | 2004-10-22 | 2010-10-29 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
US7645755B2 (en) | 2004-10-22 | 2010-01-12 | Janssen Pharmaceutical N.V. | Inhibitors of c-fms kinase |
US20060281700A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminopyrimidines kinase modulators |
US20060281788A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
US20060281771A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminoquinoline and aminoquinazoline kinase modulators |
US20060281769A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators |
US20060281755A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminopyrimidines kinase modulators |
BRPI0617489A2 (en) | 2005-10-18 | 2011-07-26 | Janssen Pharmaceutica Nv | compounds, composition and use of said compounds to inhibit flt3 kinase |
US8697716B2 (en) | 2006-04-20 | 2014-04-15 | Janssen Pharmaceutica Nv | Method of inhibiting C-KIT kinase |
ES2565238T3 (en) | 2006-04-20 | 2016-04-01 | Janssen Pharmaceutica N.V. | C-fms kinase inhibitors |
MX2008013532A (en) | 2006-04-20 | 2009-01-15 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase. |
PT2021335E (en) | 2006-04-20 | 2011-07-25 | Janssen Pharmaceutica Nv | Heterocyclic compounds as inhibitors of c-fms kinase |
JP2008122527A (en) | 2006-11-09 | 2008-05-29 | Nec Electronics Corp | Optical transceiver module and its manufacturing method |
KR101517254B1 (en) * | 2007-06-01 | 2015-04-30 | 바스프 에스이 | Method for the production of n-substituted (3-dihalomethyl-1-methyl-pyrazole-4-yl)carboxamides |
EP2048126A1 (en) * | 2007-10-11 | 2009-04-15 | Bayer Schering Pharma AG | Benzocycloheptane derivatives as selectively active oestrogens |
JO3240B1 (en) | 2007-10-17 | 2018-03-08 | Janssen Pharmaceutica Nv | Inhibitors of c-fms Kinase |
JP2011502266A (en) | 2007-10-31 | 2011-01-20 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Biomarkers to assess response to FMS treatment |
BR112012017310A2 (en) * | 2010-01-15 | 2016-04-19 | Janssen Pharmaceuticals Inc | substituted triazole derivatives as gamma secretase modulators |
JP5789259B2 (en) * | 2010-07-16 | 2015-10-07 | 協和発酵キリン株式会社 | Nitrogen-containing aromatic heterocyclic derivatives |
-
2012
- 2012-08-07 JO JOP/2018/0012A patent/JOP20180012A1/en unknown
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2013
- 2013-08-05 IN IN660DEN2015 patent/IN2015DN00660A/en unknown
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- 2013-08-05 JP JP2015526603A patent/JP6290884B2/en active Active
- 2013-08-05 CN CN201380041841.0A patent/CN104520295B/en active Active
- 2013-08-05 US US13/959,158 patent/US9029352B2/en active Active
- 2013-08-05 CN CN201710504413.7A patent/CN107266405A/en active Pending
- 2013-08-05 EP EP13748242.8A patent/EP2882744B8/en active Active
- 2013-08-05 ES ES16172842.3T patent/ES2658773T3/en active Active
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- 2013-08-05 ES ES13748242.8T patent/ES2607807T3/en active Active
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- 2013-08-06 TW TW106125831A patent/TWI646090B/en active
- 2013-08-06 JO JOP/2013/0237A patent/JO3248B1/en active
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2015
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AU2017201415B2 (en) | 2019-01-03 |
TWI646090B (en) | 2019-01-01 |
UY34972A (en) | 2014-02-28 |
TW201741292A (en) | 2017-12-01 |
JP6290884B2 (en) | 2018-03-07 |
JP2015524471A (en) | 2015-08-24 |
ES2658773T3 (en) | 2018-03-12 |
JO3248B1 (en) | 2018-09-16 |
TWI608004B (en) | 2017-12-11 |
CN104520295B (en) | 2017-07-18 |
EP3091006A1 (en) | 2016-11-09 |
CN104520295A (en) | 2015-04-15 |
ES2607807T3 (en) | 2017-04-04 |
AU2013299926B2 (en) | 2017-06-01 |
EP2882744B1 (en) | 2016-09-21 |
US9029352B2 (en) | 2015-05-12 |
US20150232439A1 (en) | 2015-08-20 |
AU2013299926A1 (en) | 2015-05-21 |
EP2882744A1 (en) | 2015-06-17 |
EP3091006B1 (en) | 2018-01-17 |
CN107266405A (en) | 2017-10-20 |
HK1209418A1 (en) | 2016-04-01 |
IN2015DN00660A (en) | 2015-06-26 |
EP2882744B8 (en) | 2016-11-09 |
WO2014025679A1 (en) | 2014-02-13 |
AR092070A1 (en) | 2015-03-18 |
AR117002A2 (en) | 2021-06-30 |
US20140045789A1 (en) | 2014-02-13 |
HK1210616A1 (en) | 2016-04-29 |
TW201408664A (en) | 2014-03-01 |
AU2017201415A1 (en) | 2017-03-16 |
AU2017201415C1 (en) | 2019-05-23 |
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